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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2081329생성일: 2026년 10월 26일

Carbon Dioxide → 4-methoxy-2-(trifluoromethyl)benzoic Acid

https://huagongshe.com/reaction/2081329

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Hydrochloric AcidHCID 313—
반응물IodineHCID 807—
반응물MagnesiumHCID 5462224—
반응물1-Bromo-4-methoxy-2-(trifluoromethyl)benzeneHCID 14484727—
용매TetrahydrofuranHCID 8028—
생성물4-methoxy-2-(trifluoromethyl)benzoic AcidHCID 277529439.5%

반응 단계

Dry tetrahydrofuran (10 ml) was added to 3-trifluoromethyl-4-bromo-1-methoxybenzene (compound III) (4.4 g) and metallic magnesium (0.41 g) and thereto was further added a catalytic amount of iodine, followed by refluxing for 1.5 hours with stirring. After the temperature was returned to room temperature, to the mixture was slowly added dropwise a solution prepared by adding dry ice (30 g) to dry tetrahydrofuran (10 ml) at -40° C. or lower. The temperature was returned to room temperature and then the reaction was allowed to proceed for further 2 hours. Then, the reaction mixture was added to 1N hydrochloric acid (50 ml) to stop the reaction and repeatedly extracted with ethyl acetate. The ethyl acetate layer was sufficiently washed with water and dried by adding anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure and then, the resulting solid was recrystallized from methylene chloride to obtain 2-trifluoromethyl-4-methoxybenzoic acid (compound IV, 1.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05183934
출처 데이터셋uspto-grants-1993_02
ORD IDord-314b0b1b98fc45a1b20a8bf062c2018f
출처 메모uspto-grants-1993_02